Reaktionsgleichung
[C:1]([O:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][O:10][C:11]1[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=1)[CH:14]=O)(=[O:3])[CH3:2].C1(P(=[CH:38][C:39]([O:41][CH3:42])=[O:40])(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>>[CH3:42][O:41][C:39](=[O:40])/[CH:38]=[CH:14]/[C:13]1[CH:16]=[CH:17][CH:18]=[C:11]([O:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][O:4][C:1](=[O:3])[CH3:2])[CH:12]=1Komponenten
3
Versuchsvorschrift
Using the procedure of example 28, the title compound was prepared in 80% yield, from 2.6 g (10.4 mmol) of 3-[[5-(acetyloxy)pentyl]oxy]benzaldehyde and 4.0 g (12 mmol) of methyl (triphenylphosphoranylidene)acetate, as a colorless solid, mp 65°-67° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-c8004816dd8c4c1d97d0f74f3500c462
- Quelldatensatz
- uspto-grants-1993_12
- Patentnummer
- US05273999
Verknüpfte Notizen
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